A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406021



Internal ID21063574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:105121090..105698274hg38UCSC Ensembl
chr5:104456791..105033975hg19UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg38577185
hg19577185
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406021
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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